(Q30467776)

11 August 2017

Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS) (English)

1 reference

11 August 2017

Shin-ichi Usami

1

1 reference

11 August 2017

Maiko Miyagawa

2

1 reference

11 August 2017

Shin-ya Nishio

3

1 reference

11 August 2017

Hideaki Moteki

4

1 reference

11 August 2017

Yutaka Takumi

5

1 reference

11 August 2017

Mika Suzuki

6

1 reference

11 August 2017

Yoko Kitano

7

1 reference

11 August 2017

Satoshi Iwasaki

8

1 reference

11 August 2017

language of work or name

English

0 references

publication date

1 April 2012

1 reference

11 August 2017

Acta Oto-Laryngologica

1 reference

11 August 2017

132

1 reference

11 August 2017

4

1 reference

11 August 2017

377-384

1 reference

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region.

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Cadherin 23 is a component of the tip link in hair-cell stereocilia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Sensorineural hearing loss associated with the mitochondrial mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Prevalent connexin 26 gene (GJB2) mutations in Japanese

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Prevalence of mitochondrial gene mutations among hearing impaired patients

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Objective evaluation of aided thresholds using auditory steady-state responses.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335139

Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.

20 June 2018

1 reference

https://api.crossref.org/works/10.3109%2F00016489.2011.649493

Validation of the LittlEARS((R)) Auditory Questionnaire in children with normal hearing

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00016489.2011.649493

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00016489.2011.649493

Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00016489.2011.649493

Cochlear implantation in individuals with Usher type 1 syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22443853

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3109/00016489.2011.649493

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

22443853

1 reference